USP53
Disease associated variation - GWASdb
ChrPosSNP ID(dbSNP 142)RefAltOri SNP IDP-valueDrug NameDrug AnnoGWAS TraitHPO IDDO IDAATypeTrait or Drug
4120151012rs9996382AGrs99963821.81E-04Type 2 diabetesHPOID:0005978DOID:9352GintronGWASdb_trait
4120151452rs10031033TCrs100310332.85E-04Type 2 diabetesHPOID:0005978DOID:9352TintronGWASdb_trait
4120159334rs11944880CTrs119448805.41E-04Multiple complex diseasesHPOID:0000118NACintronGWASdb_trait
4120167111rs7356185TCrs73561850.000141Coronary artery diseaseHPOID:0001677DOID:3393CintronGWASdb_trait
4120187611rs11098499CTrs110984999.00E-06Corneal astigmatismHPOID:0000483DOID:10124CintronGWASdb_trait
4120214030rs3749591TGrs37495919.85E-04Glycosylated haemoglobin levelsHPOID:0011902|HPOID:0000077|HPOID:0001626|HPOID:0000819|HPOID:0000479DOID:1287|DOID:9351|DOID:557|DOID:5679TmissenseGWASdb_trait